In vitro method for teaching percutaneous vascular catheterization.

1991 ◽  
Vol 157 (5) ◽  
pp. 1125-1125
Author(s):  
D J Eschelman ◽  
A J Greenfield ◽  
D T Gibbens
1979 ◽  
Vol 41 (03) ◽  
pp. 576-582
Author(s):  
A R Pomeroy

SummaryThe limitations of currently used in vitro assays of heparin have demonstrated the need for an in vivo method suitable for routine use.The in vivo method which is described in this paper uses, for each heparin preparation, four groups of five mice which are injected intravenously with heparin according to a “2 and 2 dose assay” procedure. The method is relatively rapid, requiring 3 to 4 hours to test five heparin preparations against a standard preparation of heparin. Levels of accuracy and precision acceptable for the requirements of the British Pharmacopoeia are obtained by combining the results of 3 to 4 assays of a heparin preparation.The similarity of results obtained the in vivo method and the in vitro method of the British Pharmacopoeia for heparin preparations of lung and mucosal origin validates this in vivo method and, conversely, demonstrates that the in vitro method of the British Pharmacopoeia gives a reliable estimation of the in vivo activity of heparin.


1986 ◽  
Vol 5 (4) ◽  
pp. 309-317 ◽  
Author(s):  
Paul S. Imperia ◽  
Hillard M. Lazarus ◽  
Roberte Botti ◽  
Jonathan H. Lass
Keyword(s):  

2010 ◽  
Vol 87 (4) ◽  
pp. 363-369 ◽  
Author(s):  
Robert L. Magaletta ◽  
Suzanne N. DiCataldo ◽  
Dong Liu ◽  
Hong Laura Li ◽  
Rajendra P. Borwankar ◽  
...  

2018 ◽  
Vol 14 (5) ◽  
pp. 458-464 ◽  
Author(s):  
Graciela Granados-Guzmán ◽  
Rocio Castro-Rios ◽  
Noemi Waksman de Torres ◽  
Ricardo Salazar-Aranda

1985 ◽  
Vol 76 (2) ◽  
pp. 375-382 ◽  
Author(s):  
Mary Rusckowski ◽  
Paul W. Doherty ◽  
Frank Virzi ◽  
Donald J. Hnatowich

1980 ◽  
Vol 26 (2) ◽  
pp. 272-274 ◽  
Author(s):  
L. L. Barton ◽  
E. W. Foster ◽  
G. V. Johnson

An in vitro method for detecting toxin produced by Aphanizomenon flos-aquae is described. This procedure is more sensitive than the mouse toxicity test and is based on viability changes in human leukocytes.


1999 ◽  
Vol 86 (1) ◽  
pp. 133-138 ◽  
Author(s):  
Hideo Ikarugi ◽  
Tomomi Taka ◽  
Shoko Nakajima ◽  
Takanori Noguchi ◽  
Sadahiro Watanabe ◽  
...  

The effects of exercise and catecholamines on platelet reactivity or coagulation and fibrinolysis appear to be inconsistent. This may be partly due to the methods employed in previous studies. In the present study, we investigated the effects of acute aerobic exercise and catecholamines on the thrombotic status by a novel in vitro method, shear-induced hemostatic plug formation (hemostatometry), using nonanticoagulated (native) blood. Aerobic exercise (60% maximal O2consumption) was performed by healthy male volunteers for 20 min, and the effect on platelet reactivity and coagulation was assessed by performing hemostatometry before and immediately after exercise. Exercise significantly increased shear-induced platelet reactivity, coagulation, and catecholamine levels. The effect of catecholamines on platelet reactivity and coagulation was assessed in vitro by adding catecholamines to blood collected in the resting state. The main findings of the present study are that elevation of circulating norepinephrine at levels that are attained during exercise causes platelet hyperreactivity and a platelet-mediated enhanced coagulation. This may be a mechanism of an association of aerobic exercise with thrombotic risk.


Sign in / Sign up

Export Citation Format

Share Document